Potassium Carbonate → 2-bromo-6-hydroxy-1H-indenone
Reaction equation
[Br:1][C:2]1[C:3](=[O:11])[C:4]2[C:9]([CH:10]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2.C([O-])([O-])=[O:13].[K+].[K+]>CO>[Br:1][C:2]1[C:3](=[O:11])[C:4]2[C:9]([CH:10]=1)=[CH:8][CH:7]=[C:6]([OH:13])[CH:5]=2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1 to 1.2 eq of the 2-bromo-1H-indenone prepared in Step 4 is dissolved in MeOH, and then K2CO3 (1 to 2 eq) is added thereto. The resulting mixture is stirred at room temperature for 2 to 7 h, to obtain the 2-bromo-6-hydroxy-1H-indenone of formula 8 in which acetyl group is removed.
Sources & evidence
- ORD record
- ord-65de89de0233422f994a3a1f0108cdff
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08877747B2
Reaction notes
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